Medication info
Carvedilol Tablets 12.5 mg (Carvedilol)

Carvedilol Tablets 12.5 mg (Carvedilol)

Prescription medicationTabletOral
Ingredient · strength
Carvedilol›12.5mg / 1 tablet
Manufacturer / importer
IYun Pharmaceutical Co., Ltd.
Appearance
Reddish-brown round tablets
Packaging
90 tablets (10 tablets/PTP X 9)
Approval status
Active

MFDS item code 201908436 · Approved 2019.12.16 · Insurance code 658604690

Summary

Main use
Adjunctive treatment of congestive heart failure, and treatment of essential hypertension and chronic stable angina
Who takes it
Adults
Adult dose
Do not increase the dose or stop taking this medicine without your doctor’s instructions. 1. Essential hypertension 1) Adults (1) For the first 2 days, administer 12.5 mg of carvedilol orally once daily, then administer 25 mg orally once daily. (2) The usual dose is 25 mg orally once daily for 2 weeks. If a dose increase is needed, increase to 25 mg twice daily. The maximum dose per administration is 25 mg, and the maximum daily dose is 50 mg. 2) Elderly patients In some elderly patients, 12.5 mg once daily may be sufficiently effective. However, the dose may be increased if the effect is insufficient after 2 weeks of treatment. 2. Chronic stable angina 1) For the first 2 days, administer 12.5 mg of this medicine orally twice daily, then administer 25 mg orally twice daily. 2) The usual dose is 25 mg twice daily for 2 weeks. If a dose increase is needed (excluding elderly patients), the dose may be increased to 50 mg twice daily. 3. Congestive heart failure Before starting treatment with this medicine, the patient’s existing standard treatment regimen (the conventional treatment regimen for chronic heart failure, consisting of an ACE inhibitor, a diuretic, and usually a digitalis preparation) should be stable. Fluid retention should also be minimized before starting treatment with this medicine. 1) The usual initial treatment is 3.125 mg of this medicine orally twice daily for 2 weeks. If the patient tolerates this treatment well, increase the dose to 6.25 mg twice daily for 2 weeks, then to 12.5 mg twice daily for 2 weeks, and then to 25 mg twice daily. 2) After taking each dose for at least 2 weeks, increase the dose gradually to the dose tolerated by the patient. 3) The minimum effective dose is 6.25 mg twice daily. The maximum dose is 25 mg twice daily for patients weighing 85 kg or less, and 50 mg twice daily for patients weighing more than 85 kg. 4) To control the rate of absorption, it is recommended to take the medicine with meals in the morning and evening. Taking it with meals slows absorption and may reduce the incidence of orthostatic hypotension.

Ingredients

Manufacturer
IYun Pharmaceutical Co., Ltd.

Efficacy & effects

Adjunctive treatment of congestive heart failure, and treatment of essential hypertension and chronic stable angina

  • Essential hypertension
  • chronic stable angina
  • congestive heart failure
View approved original text

This medication is used for cardiovascular diseases such as essential hypertension, chronic stable angina, and congestive heart failure. Additionally, it is administered as an adjunct therapy in conjunction with diuretics, digitalis preparations, ACE inhibitors, and other vasodilators to help improve symptoms. It is utilized in the treatment of various heart-related conditions.

How to take

Adult dose

Do not increase the dose or stop taking this medicine without your doctor’s instructions. 1. Essential hypertension 1) Adults (1) For the first 2 days, administer 12.5 mg of carvedilol orally once daily, then administer 25 mg orally once daily. (2) The usual dose is 25 mg orally once daily for 2 weeks. If a dose increase is needed, increase to 25 mg twice daily. The maximum dose per administration is 25 mg, and the maximum daily dose is 50 mg. 2) Elderly patients In some elderly patients, 12.5 mg once daily may be sufficiently effective. However, the dose may be increased if the effect is insufficient after 2 weeks of treatment. 2. Chronic stable angina 1) For the first 2 days, administer 12.5 mg of this medicine orally twice daily, then administer 25 mg orally twice daily. 2) The usual dose is 25 mg twice daily for 2 weeks. If a dose increase is needed (excluding elderly patients), the dose may be increased to 50 mg twice daily. 3. Congestive heart failure Before starting treatment with this medicine, the patient’s existing standard treatment regimen (the conventional treatment regimen for chronic heart failure, consisting of an ACE inhibitor, a diuretic, and usually a digitalis preparation) should be stable. Fluid retention should also be minimized before starting treatment with this medicine. 1) The usual initial treatment is 3.125 mg of this medicine orally twice daily for 2 weeks. If the patient tolerates this treatment well, increase the dose to 6.25 mg twice daily for 2 weeks, then to 12.5 mg twice daily for 2 weeks, and then to 25 mg twice daily. 2) After taking each dose for at least 2 weeks, increase the dose gradually to the dose tolerated by the patient. 3) The minimum effective dose is 6.25 mg twice daily. The maximum dose is 25 mg twice daily for patients weighing 85 kg or less, and 50 mg twice daily for patients weighing more than 85 kg. 4) To control the rate of absorption, it is recommended to take the medicine with meals in the morning and evening. Taking it with meals slows absorption and may reduce the incidence of orthostatic hypotension.

Precautions

This medication should not be administered to certain patients. For instance, it may be dangerous for those with allergies to this medication or its components, cardiac shock, heart conduction disturbances, cor pulmonale, diabetic ketoacidosis, severely impaired cardiac function, asthma, or chronic lung disease. It is also advisable for pregnant or breastfeeding women not to use this medication. Patients with genetic issues such as lactose intolerance should also avoid taking it. Care should be taken with patients who have diabetes, a history of hypersensitivity, heart disease, impaired kidney or liver function, elderly patients, etc., as there may be an increased potential for symptom worsening or side effects. The medication should be taken carefully under the guidance of a physician. This medication may cause various side effects such as dizziness, headache, fatigue, reduced heart rate, lowered blood pressure, worsening heart failure, gastrointestinal symptoms, skin rashes, etc. If any abnormal symptoms occur, immediate consultation with medical personnel is necessary. Regular monitoring of cardiac function tests, blood pressure, pulse, liver and kidney functions is important when taken long-term. Suddenly stopping the medication may worsen symptoms, so the dose should be gradually reduced according to a physician's instructions. This medication may interact with other drugs, so care should be taken particularly when taken together with antihypertensives, antidepressants, antiarrhythmics, insulin, alcohol, etc. All medications being taken should be disclosed to the doctor or pharmacist. Pregnant or breastfeeding individuals should not take this medication, and its safety in children and adolescents has not been established, so its use is not recommended. In case of overdose, severe symptoms such as pronounced hypotension, decreased heart rate, heart failure, and respiratory distress may occur, and immediate contact with medical institutions is necessary for appropriate treatment. This medication may discolor due to light, so it should be stored in a sealed container that blocks light, kept away from direct sunlight, and stored out of reach of children, without being transferred to another container.

Side effects

  • Dizziness
  • headache
  • fatigue
  • weakness
  • hallucination
  • confusion
  • depression
  • sleep disorder
  • nightmares
  • mental illness
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  • severe bradycardia
  • shock
  • complete atrioventricular block
  • heart failure
  • cardiac arrest
  • significant drop in blood pressure
  • loss of consciousness
  • decreased pulse rate
  • cold limbs
  • edema
  • asystole
  • worsening kidney function
  • renal failure
  • increased respiratory resistance
  • nausea
  • diarrhea
  • abdominal pain
  • vomiting
  • constipation
  • urticaria
  • itching
  • lichenoid reaction
  • hyperhidrosis
  • allergic rash
  • serum aminotransferase changes
  • thrombocytopenia
  • leukopenia
  • onset of latent diabetes
  • hyperglycemia
  • weight gain
  • increased blood cholesterol
  • bradycardia
  • hypotension
  • breathlessness
  • hypertension in angina
  • liver dysfunction
  • jaundice
  • limb pain
  • decreased tear production
  • sensory disturbances
  • visual disturbances
  • eye irritation
  • dry mouth
  • urination disorders
  • sexual dysfunction
  • allergic reactions
  • toxic epidermal necrolysis
  • Stevens-Johnson syndrome
  • marked drop in blood pressure
  • slowed heartbeat
  • myocardial weakness
  • asystole
  • dyspnea
  • bronchospasm
  • vomiting
  • consciousness disorders
  • generalized seizures

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a sealed container that can block light and kept at room temperature between 1 to 30 degrees Celsius. Storing it this way will maintain the effectiveness of the medication and prevent degradation.

Appearance and packaging

Appearance

Reddish-brown round tablets

Package unit

90 tablets (10 tablets/PTP X 9)

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.